Product NDC: | 0603-0746 |
Proprietary Name: | Doc Q Lace |
Non Proprietary Name: | Docusate sodium |
Active Ingredient(s): | 10 mg/mL & nbsp; Docusate sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-0746 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part334 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19901005 |
Package NDC: | 0603-0746-58 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0603-0746-58) |
NDC Code | 0603-0746-58 |
Proprietary Name | Doc Q Lace |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (0603-0746-58) |
Product NDC | 0603-0746 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Docusate sodium |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19901005 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | DOCUSATE SODIUM |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes |